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A comprehensive framework for evaluation of high pacing frequency and arrhythmic optical mapping signals

Introduction: High pacing frequency or irregular activity due to arrhythmia produces complex optical mapping signals and challenges for processing. The objective is to establish an automated activation time-based analytical framework applicable to optical mapping images of complex electrical behavio...

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Autores principales: Ramlugun, Girish S., Kulkarni, Kanchan, Pallares-Lupon, Nestor, Boukens, Bastiaan J., Efimov, Igor R., Vigmond, Edward J., Bernus, Olivier, Walton, Richard D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9901579/
https://www.ncbi.nlm.nih.gov/pubmed/36755791
http://dx.doi.org/10.3389/fphys.2023.734356
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author Ramlugun, Girish S.
Kulkarni, Kanchan
Pallares-Lupon, Nestor
Boukens, Bastiaan J.
Efimov, Igor R.
Vigmond, Edward J.
Bernus, Olivier
Walton, Richard D.
author_facet Ramlugun, Girish S.
Kulkarni, Kanchan
Pallares-Lupon, Nestor
Boukens, Bastiaan J.
Efimov, Igor R.
Vigmond, Edward J.
Bernus, Olivier
Walton, Richard D.
author_sort Ramlugun, Girish S.
collection PubMed
description Introduction: High pacing frequency or irregular activity due to arrhythmia produces complex optical mapping signals and challenges for processing. The objective is to establish an automated activation time-based analytical framework applicable to optical mapping images of complex electrical behavior. Methods: Optical mapping signals with varying complexity from sheep (N = 7) ventricular preparations were examined. Windows of activation centered on each action potential upstroke were derived using Hilbert transform phase. Upstroke morphology was evaluated for potential multiple activation components and peaks of upstroke signal derivatives defined activation time. Spatially and temporally clustered activation time points were grouped in to wave fronts for individual processing. Each activation time point was evaluated for corresponding repolarization times. Each wave front was subsequently classified based on repetitive or non-repetitive events. Wave fronts were evaluated for activation time minima defining sites of wave front origin. A visualization tool was further developed to probe dynamically the ensemble activation sequence. Results: Our framework facilitated activation time mapping during complex dynamic events including transitions to rotor-like reentry and ventricular fibrillation. We showed that using fixed AT windows to extract AT maps can impair interpretation of the activation sequence. However, the phase windowing of action potential upstrokes enabled accurate recapitulation of repetitive behavior, providing spatially coherent activation patterns. We further demonstrate that grouping the spatio-temporal distribution of AT points in to coherent wave fronts, facilitated interpretation of isolated conduction events, such as conduction slowing, and to derive dynamic changes in repolarization properties. Focal origins precisely detected sites of stimulation origin and breakthrough for individual wave fronts. Furthermore, a visualization tool to dynamically probe activation time windows during reentry revealed a critical single static line of conduction slowing associated with the rotation core. Conclusion: This comprehensive analytical framework enables detailed quantitative assessment and visualization of complex electrical behavior.
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spelling pubmed-99015792023-02-07 A comprehensive framework for evaluation of high pacing frequency and arrhythmic optical mapping signals Ramlugun, Girish S. Kulkarni, Kanchan Pallares-Lupon, Nestor Boukens, Bastiaan J. Efimov, Igor R. Vigmond, Edward J. Bernus, Olivier Walton, Richard D. Front Physiol Physiology Introduction: High pacing frequency or irregular activity due to arrhythmia produces complex optical mapping signals and challenges for processing. The objective is to establish an automated activation time-based analytical framework applicable to optical mapping images of complex electrical behavior. Methods: Optical mapping signals with varying complexity from sheep (N = 7) ventricular preparations were examined. Windows of activation centered on each action potential upstroke were derived using Hilbert transform phase. Upstroke morphology was evaluated for potential multiple activation components and peaks of upstroke signal derivatives defined activation time. Spatially and temporally clustered activation time points were grouped in to wave fronts for individual processing. Each activation time point was evaluated for corresponding repolarization times. Each wave front was subsequently classified based on repetitive or non-repetitive events. Wave fronts were evaluated for activation time minima defining sites of wave front origin. A visualization tool was further developed to probe dynamically the ensemble activation sequence. Results: Our framework facilitated activation time mapping during complex dynamic events including transitions to rotor-like reentry and ventricular fibrillation. We showed that using fixed AT windows to extract AT maps can impair interpretation of the activation sequence. However, the phase windowing of action potential upstrokes enabled accurate recapitulation of repetitive behavior, providing spatially coherent activation patterns. We further demonstrate that grouping the spatio-temporal distribution of AT points in to coherent wave fronts, facilitated interpretation of isolated conduction events, such as conduction slowing, and to derive dynamic changes in repolarization properties. Focal origins precisely detected sites of stimulation origin and breakthrough for individual wave fronts. Furthermore, a visualization tool to dynamically probe activation time windows during reentry revealed a critical single static line of conduction slowing associated with the rotation core. Conclusion: This comprehensive analytical framework enables detailed quantitative assessment and visualization of complex electrical behavior. Frontiers Media S.A. 2023-01-23 /pmc/articles/PMC9901579/ /pubmed/36755791 http://dx.doi.org/10.3389/fphys.2023.734356 Text en Copyright © 2023 Ramlugun, Kulkarni, Pallares-Lupon, Boukens, Efimov, Vigmond, Bernus and Walton. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Ramlugun, Girish S.
Kulkarni, Kanchan
Pallares-Lupon, Nestor
Boukens, Bastiaan J.
Efimov, Igor R.
Vigmond, Edward J.
Bernus, Olivier
Walton, Richard D.
A comprehensive framework for evaluation of high pacing frequency and arrhythmic optical mapping signals
title A comprehensive framework for evaluation of high pacing frequency and arrhythmic optical mapping signals
title_full A comprehensive framework for evaluation of high pacing frequency and arrhythmic optical mapping signals
title_fullStr A comprehensive framework for evaluation of high pacing frequency and arrhythmic optical mapping signals
title_full_unstemmed A comprehensive framework for evaluation of high pacing frequency and arrhythmic optical mapping signals
title_short A comprehensive framework for evaluation of high pacing frequency and arrhythmic optical mapping signals
title_sort comprehensive framework for evaluation of high pacing frequency and arrhythmic optical mapping signals
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9901579/
https://www.ncbi.nlm.nih.gov/pubmed/36755791
http://dx.doi.org/10.3389/fphys.2023.734356
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